Tag | Content |
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EnhancerAtlas ID | HS133-20462 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr21:33968720-33970480 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr21:33968810-33968825 | GAGGTCAGGAGTTCA | + | 6.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr21 | 33969151 | 33969267 | chr21 | 33969328 | 33969937 |
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| Number: 1 | ID | Chromosome | Start | End |
GH21I032596 | chr21 | 33969053 | 33970477 |
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Enhancer Sequence | AACATTTAAG AGTGTACCAC TATCATGGCC AGGCACGGTG GCTCACGCCT GTAATCCCAG 60 CACTTTGGGA GGCTGAGGTG GGTGGATCAT GAGGTCAGGA GTTCAAGACC AGCCTGGCCA 120 AGATGGTGAA ACCCCATCTC TACTAAAAAT ACAAAAATTA GCCAGGTATG GTGGGGGGTG 180 CTTGTAATCC CAGTTACTTG AGAGGCTGAG GCAGAGAATT GCTTGAACCC GGGAGGCAGA 240 GATTGCAGTG AGCCGAGATC GCACCACTGC ACTCCAGCCT GGGGGGTGAC AGATTGAGAC 300 TCTGTCTCAA AAAAAAAAAA AAAAAAAAAA AATTAAAAGA GCGTACCACT ATCTACATAA 360 ATACATACAC TGAAAATGCA TAATAACTTC AGCTGCTCTG ATACCAAATG CCAACATCCA 420 TGAAAATGTC CTACAAGAGA GGGAGGGAGC TGCATCAATT GCGCTGATGA CCCTGGGCCA 480 ATTGTCCTAA GATCTGTTAG GTCTGTGATC TGGGAGGGCC CTGGAGATCC TGAGGCAGCA 540 GGTGAGGCCT GAGGCCTGGG ACCCCAAACC CAGCTAAAAC TAAAAACTAA AAACTCTTAA 600 GTGTAGAGTT CAGTGATACT CACATTCTTG TGCAACCATC AGCACCATCC ATCTCCAGAA 660 TGTTTTTATC TTCTCAAACT TAAACTCTAT ACCCATTAAA CAGTAACTCT CCATCCTTCC 720 CTGCTGTCCC CAGCCCCTAA CAACCATCAT TCTGCTTTGT CTCTGGATCT GACTACTCTA 780 GGAACCTCGT ATAAGTGGAA TCTTACAGTA TTTGTCATTT GGTATCTGGC TTATTTCACT 840 CAGTGTAATG TCATCAAGGT TCATCCCTGT TGGAGCATGT GTCAGGATTC CCTTCCGTTG 900 TAAGGCTGAA TAATATTCCA TTGTACGGAT ACACCACCTC TTGTTGACTC ATTCATCCTC 960 TTGTTGACTC ATTCATCTGT GGATGGGCAC TTGGGTTGCC TCCACGTTTG AGTTATTGTG 1020 AATCATGCTG CCGTGGACGT GGCTGTACTG CAACTGGTTT TGCATTTATT TGAATAGGTG 1080 GATTTCAAAG GTACAAAAGA CCATCCTGTG AACCGTGACT CCCTCCCAGC CCATCCTCCA 1140 GGCCCCCTAG AGTTTTAACC ACAAGCAGCC ATGGTCACCA GTTTCTTGTG ATCTTTCTAA 1200 GAGTATGTGA GCATATGTGC TATGCCATGG TAGAGGCTGG ACGCGGTGGC TCACGCCTGT 1260 AATCCCAACA CTTTGGGAGG CTGAGGCAGG CAGATCACCT GAGGTTGGGA GTGAGACCAG 1320 CCTGGCCAAT ACGGTGAAAC CCTGCCTTCA CTAAAAATAC TAAAATTAGT CGGGCACAGT 1380 GGTGCGTGCC TGCAATCCCA GCTACTCAGG AGGCTGAGGC AGGAGAACAG CTTGAACCCG 1440 GGAGGTGGAG GTTGCAGTGA GCCAAGATCA TGCCACTGCA CTCCAGCCTG GGTAACAGAG 1500 TGAGACCCTG TCTCAAAATA AACAAACAAA TAAATACAAT AAAATTAAAA ATCTAACAAC 1560 AGTGCCCTCG TTCCCATGAT CTCACAGTCC ATCCAGGGAG ACAGACTTGT AACCGAATGC 1620 CATGATTACA ACCAGCTCAA TGGGAGATGA AGAAGGAGGT GTGTTCGGAA ACCTGGGAAC 1680 TGAGGAGGGA GTGGGCTCTC AACCTTAACA TGGGCTGCGG GAGTTGGGCA AGAATCAGAA 1740 ACAGATTATG TAGATGATAC 1760
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